Reacción #1483064

ord-f89e4aa913364b80a1682c35f5efeb5f

Ecuación de reacción

O=C(O)c1ccc2[nH]ccc2c1
1H-indole-5-carboxylic acid
[H-].[Na+]
sodium hydride
CI
iodomethane
CN(C)C=O
DMF
COC(=O)c1ccc2c(ccn2C)c1
1-methyl-1H-indole-5-carboxylic acid methyl ester
Rendimiento 93.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was then quenched with water (5 mL)
  2. 2
    workup.ADDITIONdiluted with ether (150 mL) and ethyl acetate (50 mL)
  3. 3
    LavadoAfter washing with aq. NH4Cl (100 mL), water (100 mL)
  4. 4
    Secadobrine (100 mL), the organic layer was dried over MgSO4
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated

Procedimiento

A solution of 1H-indole-5-carboxylic acid (1.6 g, 10 mmol), sodium hydride (1.2 g, 30 mmol), iodomethane (6.2 mL, 100 mmol) and DMF (40 mL) was stirred and room temperature for 24 hr. The reaction mixture was then quenched with water (5 mL) and diluted with ether (150 mL) and ethyl acetate (50 mL). After washing with aq. NH4Cl (100 mL), water (100 mL) and then brine (100 mL), the organic layer was dried over MgSO4, filtered and concentrated. The remaining material was subjected to flash chromatography (ethyl acetate/hexane 1:4) to provide 1-methyl-1H-indole-5-carboxylic acid methyl ester as a crystalline solid (1.77 g, 93% yield). 1H NMR (400 MHz, CDCl3) δ 8.40 (s, 1H), 7.94 (d, 1H, J=9.0 Hz), 7.34 (d, 1H, J=9.0 Hz), 7.12 (d, 1H, J=2.9 Hz), 6.60 (d, 1H, J=2.9 Hz), 3.94 (s, 3H), 3.83 (s, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08900565B2uspto-grants-2014_12